US4764201A - Plant growth regulation - Google Patents

Plant growth regulation Download PDF

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US4764201A
US4764201A US06/712,751 US71275185A US4764201A US 4764201 A US4764201 A US 4764201A US 71275185 A US71275185 A US 71275185A US 4764201 A US4764201 A US 4764201A
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menadiol
vitamin
water
compound
plants
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US06/712,751
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Yasuo Iino
Yoshinori Saito
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Tomoe Kagaku Kogyo KK
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Tomoe Kagaku Kogyo KK
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Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N49/00—Biocides, pest repellants or attractants, or plant growth regulators, containing compounds containing the group, wherein m+n>=1, both X together may also mean —Y— or a direct carbon-to-carbon bond, and the carbon atoms marked with an asterisk are not part of any ring system other than that which may be formed by the atoms X, the carbon atoms in square brackets being part of any acyclic or cyclic structure, or the group, wherein A means a carbon atom or Y, n>=0, and not more than one of these carbon atoms being a member of the same ring system, e.g. juvenile insect hormones or mimics thereof
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
    • A01N33/02—Amines; Quaternary ammonium compounds
    • A01N33/06—Nitrogen directly attached to an aromatic ring system
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
    • A01N33/02—Amines; Quaternary ammonium compounds
    • A01N33/08—Amines; Quaternary ammonium compounds containing oxygen or sulfur
    • A01N33/10—Amines; Quaternary ammonium compounds containing oxygen or sulfur having at least one oxygen or sulfur atom directly attached to an aromatic ring system
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/02—Saturated carboxylic acids or thio analogues thereof; Derivatives thereof
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
    • A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
    • A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
    • A01N41/04—Sulfonic acids; Derivatives thereof
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
    • A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
    • A01N57/14—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing aromatic radicals

Definitions

  • the present invention relates to the use of certain water-soluble derivatives of vitamin K compounds. More particularly, the invention relates to a method for plant growth regulation with such water-soluble derivatives of vitamin K compounds and plant growth regulating compositions comprising the same.
  • the present invention provides a method for regulating the growth of plants which comprises applying to the foliage, roots, stems, and seeds of the plants and/or to the soil or hydroponic medium in which the plants are grown an effective plant growth regulating amount of at least one water-soluble derivative of a vitamin K compound.
  • This invention further provides a plant growth regulating composition
  • a plant growth regulating composition comprising a water-soluble derivative of a vitamin K compound as an active ingredient and an agriculturally acceptable adjuvant.
  • the water-soluble derivatives of vitamin K compounds used in the present invention are known as antihemorrhagic vitamins.
  • examples of such derivatives are: menadione bisulfites such as menadione sodium bisulfite and menadione dimethylpyrimidinol bisulfite; menadiol inorganic acid ester salts such as menadiol tetrasodium diphosphate, menadiol disodium disulfate, and menadiol dipotassium disulfate; menadiol organic acid esters such as menadiol diacetate; menadiol organic acid ester salts such as menadiol dinicotinate dihydrochloride; menadiol organic acid ester quaternary ammonium salts such as menadiol bis(trimethylammonium acetate)dichloride; menadiol bis(glucoside tetraacetate); 4-amin
  • the compounds of the invention are known substances which can be easily prepared by conventional methods employed in organic chemistry. Some examples of such methods are disclosed in J. Amer. Chem. Soc., 62, 228(1940); ibid., 63, 2049(1941); ibid., 64, 2659(1942); ibid., 64, 2661(1942);U.S. Pat. No. 2,372,655; and U.S. Pat. No. 2,428,253. Further, menadione sodium bisulfite and menadione dimethylpyrimidinol bisulfite which are typical examples of the water-soluble derivatives of vitamin K compounds are available commercially and are widely used as drugs and feed additives.
  • the water-soluble derivatives of vitamin K compounds can be used singly but are ordinarily admixed with various adjuvants commonly added to agricultural chemicals including carriers, diluents, extenders and conditioning agents to form granules, wettable powders, pellets, dusts, tablets, solutions, dispersions or emulsions depending upon the purpose.
  • the proportion of the compounds of the present invention incorporated in such compositions is from 0.1 to 99.9% (by weight, as in all percentages and parts set forth hereinafter), preferably from 0.5 to 85%.
  • the carrier may be in either liquid or solid form, illustrative solid carriers being clays, talcs, diatomaceous earth, kaolin, bentonite and the like, while typical liquid carriers are water, methanol and the like.
  • ionic or nonionic surfactants high polymers such as carboxymethyl cellulose, polyvinyl alcohol and sodium alginate, and the like can be used.
  • inorganic salts inorganic fertilizers, organic fertilizers, insecticides, fungicides and herbicides may also be added to the composition or used in combination therewith.
  • the water-soluble derivatives of vitamin K compounds are applicable for the purpose of regulating the growth of a wide variety of plants.
  • plants to which the compounds of the present invention are applicable are: farm products such as rice plants, barley, wheat, oats, peas, soybeans, potatoes, sweet potatoes, and corn; vegetables such as cucumbers, eggplants, tomatoes, Chinese cabbages, Welsh onions, head lettuces, spinaches, Japanese radishes, edible burdocks, and carrots; flowers such as chrysanthemums, carnation and crocuses; trees such as cryptomeria and Japanese cypress (hinoki); lawns; and fruit trees such as mandarins, apples, pears, peaches, and grapes.
  • farm products such as rice plants, barley, wheat, oats, peas, soybeans, potatoes, sweet potatoes, and corn
  • vegetables such as cucumbers, eggplants, tomatoes, Chinese cabbages, Welsh onions, head lettuces, spinaches, Japanese radishes, edible burdocks
  • the water-soluble derivatives of vitamin K compounds can be applied at any stage of the growth of plants.
  • the compounds of the present invention may be applied at the seed stage, for example, by soaking the seed in a solution containing the compounds or coating the seed with the solution in combination with an appropriate coating agent.
  • the compounds may also be sprayed or coated over the foliage, flower or fruit of plants at the seedling stage, flowering stage or seed-setting stage thereof, or otherwise may be applied to plants sequentially at one or more stages of growth.
  • the compounds may further be applied to the soil or hydroponic medium in which plants are grown.
  • the precise rates of application of the compounds of the present invention are dependent upon the species of the plant to be treated, the specific portion of the plant to which the compounds are applied, the district in which the plant is grown, the stage of the growth of the plant, the mode of application and various other factors, so that the compounds should be applied in an appropriate rate selected with due consideration for such factors.
  • the compounds are applied at a rate of from 2 to 20,000 g per acre, preferably from 10 to 10,000 g per acre, as the effective ingredient.
  • concentration of the solution may vary in a considerably wide range, a concentration of generally from 0.001 to 100,000 ppm, preferably from 0.01 to 5,000 ppm, is employed.
  • compositions of the present invention which exhibits remarkable activity under low temperature conditions are especially noteworthy in ensuring strong resistance of seedlings to the phenomenon of lowering of season average temperatures which is observed in recent years and is called "abnormal weather conditions".
  • a liquid formulation was prepared from 5 parts of 4-amino-2-methyl-1-naphthol hydrochloride and 95 parts of water.
  • test tubes were poured menadione sodium bisulfite solutions respectively having active ingredient concentrations of 10 ppm and 100 ppm.
  • the second-leaf-stage seedlings of rice plants with the primary root thereof cut off except for the base portion 1 mm high were fixed with absorbent cotton around the stem portion thereof so that the seedlings would be disposed 1 cm below the surface of each solution.
  • the maximum root lengths of the seedlings were measured to obtain the ratios thereof to those of the untreated seedlings. The results are set forth in Table 3.
  • nursery boxes each of a size of 30 ⁇ 60 ⁇ 5 cm were filled with Pilomat® (medium for raising seedlings, supplied by Marusan Seishi K.K., Japan) as seedling beds, to which 4 g, 8 g and 16 g, respectively, of a dust formulation prepared as in Example 1 were added. Subsequently, each of the boxes was seeded with 210 g of germination-hastened paddy rice seeds (Sasanishiki) which were covered with soil for growing seedlings. The seedlings were caused to emerge at 32° C. for 2 days, greened at 25° C. for another 2 days, and then hardened in a greenhouse. 21 days after seeding, the traits of the young seedlings were examined, and the results shown in Table 4 were obtained.
  • Pilomat® medium for raising seedlings, supplied by Marusan Seishi K.K., Japan
  • 4 g, 8 g and 16 g, respectively, of a dust formulation prepared as in Example 1 were added.
  • the seedlings treated with the dust formulation of the present invention were shorter in height than the untreated seedlings but were improved in dry weight of tops and number of roots.
  • Pots each of a size of 14 cm diam. ⁇ 5 cm were filled with 500 g of garden soil each into which was injected 30 cc of a liquid formulation prepared as in Example 2 and diluted 500- and 5,000-fold, respectively. Thereafter, each of the pots was seeded with 20 seeds of Japanese radish (Ohkura Daikon) which were covered with soil. The radishes were grown in a greenhouse at 25° C. for 12 days, and the top weights thereof were measured to obtain the ratios between the weights of the treated and untreated radishes. The results are shown in Table 7.
  • Seedling cases each of a size of 5 ⁇ 15 ⁇ 10 cm were filled with 500 g of garden soil each into which was injected 30 cc of 4-amino-3-methyl-1-naphthol hydrochloride solutions having an active ingredient concentration of 10 ppm and 100 ppm, respectively. Each of the cases was then seeded with 15 seeds of spinach (Heianhiyoshimaru) which were covered with soil. The spinaches were grown in a greenhouse at 25° C. for 28 days, and the top weights thereof were measured to obtain the ratios between the weights of the treated and untreated spinaches. The results are set forth in Table 8.
  • Seedling cases each of a size of 5 ⁇ 15 ⁇ 10 cm were filled with 500 g of garden soil each into which was injected 30 cc of menadiol dinicotinate dihydrochloride solutions having an active ingredient concentration of 10 ppm and 100 ppm, respectively.
  • the cases thus treated were each seeded with 15 seeds of Chinese cabbage (Ohzeki Hakusai) which were covered with soil.
  • the Chinese cabbages were grown in a greenhouse at 25° C. for 14 days, and the top weights thereof were measured to obtain the ratios between the top weights of the treated and untreated Chinese cabbages. The results are shown in Table 9.
  • Cut chrysanthemum stalks were soaked in menadione sodium bisulfite solutions having an active ingredient concentration of 1 ppm, 10 ppm and 100 ppm, respectively, for 24 hours, then were stuck into vermiculite and were left standing in a greenhouse at 25° C. for 14 days. The rooting of the chrysanthemums was examined to obtain the ratios thereof to the rooting of the untreated chrysanthemums. The results are tabulated below.
  • Example 6 Nursery boxes each of a size of 30 ⁇ 60 ⁇ 5 cm were filled with particulate soil for raising seedlings as seedling beds, which soil was then sterilized. The procedure of Example 6 was then followed except that each of the boxes was seeded with 200 g of rice plant seeds (Koshihikari) which had been soaked in menadione dimethyl pyrimidinol bisulfite solutions having an active ingredient concentration of 10 ppm, 100 ppm and 1,000 ppm, respectively, at 20° C. for 48 hours and further treated with tap water at 32° C. for 24 hours to hasten germination. The young seedlings obtained 20 days after seeding were found to have the traits shown in the following Table 12.
  • the seed soaking treatment with menadione dimethyl pyrimidinol bisulfite solutions notably accelerates the growth of the roots of rice plants although the growth of the tops thereof was not appreciably different from that of the untreated rice plants.

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  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
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  • Pretreatment Of Seeds And Plants (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

Certain water-soluble derivatives of vitamin K compounds have been found to regulate the growth of plants. The present invention relates to a method for plant growth regulation with such water-soluble derivatives of vitamin K compounds and plant growth regulating compositions comprising the same.

Description

BACKGROUND OF THE INVENTION
The present invention relates to the use of certain water-soluble derivatives of vitamin K compounds. More particularly, the invention relates to a method for plant growth regulation with such water-soluble derivatives of vitamin K compounds and plant growth regulating compositions comprising the same.
It is highly profitable from the economical point of view to hasten the harvesttime or to enhance the yield of plants by accelerating the growth of the plants.
We have conducted intensive investigations to develop plant growth regulating compositions from among drugs, food additives, feed additives and the like which have been evaluated as innoxious. As a result, we have unexpectedly found that, by applying water-soluble derivatives of vitamin K compounds to cereals such as rice plants, a variety of garden plants such as fruit vegetables, leaf vegetables, and root vegetables, flowers and ornamental plants, and fruit trees, the growth of the shoots or tops and/or roots of the plants is notably accelerated as compared with that in the case where no such compounds are applied. On the basis of this finding, we have arrived at the present invention.
SUMMARY OF THE INVENTION
The present invention provides a method for regulating the growth of plants which comprises applying to the foliage, roots, stems, and seeds of the plants and/or to the soil or hydroponic medium in which the plants are grown an effective plant growth regulating amount of at least one water-soluble derivative of a vitamin K compound.
This invention further provides a plant growth regulating composition comprising a water-soluble derivative of a vitamin K compound as an active ingredient and an agriculturally acceptable adjuvant.
DETAILED DESCRIPTION OF THE INVENTION
The water-soluble derivatives of vitamin K compounds used in the present invention are known as antihemorrhagic vitamins. Examples of such derivatives are: menadione bisulfites such as menadione sodium bisulfite and menadione dimethylpyrimidinol bisulfite; menadiol inorganic acid ester salts such as menadiol tetrasodium diphosphate, menadiol disodium disulfate, and menadiol dipotassium disulfate; menadiol organic acid esters such as menadiol diacetate; menadiol organic acid ester salts such as menadiol dinicotinate dihydrochloride; menadiol organic acid ester quaternary ammonium salts such as menadiol bis(trimethylammonium acetate)dichloride; menadiol bis(glucoside tetraacetate); 4-amino-2 -methyl-1-naphthol hydrochloride ; 4-amino-3-methyl-1-naphthol hydrochloride; and 1,4-diamino-2-methylnaphthalene dihydrochloride.
The compounds of the invention, water-soluble derivatives of vitamin K compounds, are known substances which can be easily prepared by conventional methods employed in organic chemistry. Some examples of such methods are disclosed in J. Amer. Chem. Soc., 62, 228(1940); ibid., 63, 2049(1941); ibid., 64, 2659(1942); ibid., 64, 2661(1942);U.S. Pat. No. 2,372,655; and U.S. Pat. No. 2,428,253. Further, menadione sodium bisulfite and menadione dimethylpyrimidinol bisulfite which are typical examples of the water-soluble derivatives of vitamin K compounds are available commercially and are widely used as drugs and feed additives.
The water-soluble derivatives of vitamin K compounds, one or more thereof, can be used singly but are ordinarily admixed with various adjuvants commonly added to agricultural chemicals including carriers, diluents, extenders and conditioning agents to form granules, wettable powders, pellets, dusts, tablets, solutions, dispersions or emulsions depending upon the purpose.
The proportion of the compounds of the present invention incorporated in such compositions is from 0.1 to 99.9% (by weight, as in all percentages and parts set forth hereinafter), preferably from 0.5 to 85%.
The carrier may be in either liquid or solid form, illustrative solid carriers being clays, talcs, diatomaceous earth, kaolin, bentonite and the like, while typical liquid carriers are water, methanol and the like.
As the adjuvant for improving the dispersing, suspending, wetting, adhering and penetrating properties as well as the emulsifiability of the composition, ionic or nonionic surfactants, high polymers such as carboxymethyl cellulose, polyvinyl alcohol and sodium alginate, and the like can be used.
If necessary, other inorganic salts, inorganic fertilizers, organic fertilizers, insecticides, fungicides and herbicides may also be added to the composition or used in combination therewith.
The water-soluble derivatives of vitamin K compounds are applicable for the purpose of regulating the growth of a wide variety of plants. Among the plants to which the compounds of the present invention are applicable are: farm products such as rice plants, barley, wheat, oats, peas, soybeans, potatoes, sweet potatoes, and corn; vegetables such as cucumbers, eggplants, tomatoes, Chinese cabbages, Welsh onions, head lettuces, spinaches, Japanese radishes, edible burdocks, and carrots; flowers such as chrysanthemums, carnation and crocuses; trees such as cryptomeria and Japanese cypress (hinoki); lawns; and fruit trees such as mandarins, apples, pears, peaches, and grapes.
The water-soluble derivatives of vitamin K compounds can be applied at any stage of the growth of plants. The compounds of the present invention may be applied at the seed stage, for example, by soaking the seed in a solution containing the compounds or coating the seed with the solution in combination with an appropriate coating agent. The compounds may also be sprayed or coated over the foliage, flower or fruit of plants at the seedling stage, flowering stage or seed-setting stage thereof, or otherwise may be applied to plants sequentially at one or more stages of growth. The compounds may further be applied to the soil or hydroponic medium in which plants are grown.
The precise rates of application of the compounds of the present invention are dependent upon the species of the plant to be treated, the specific portion of the plant to which the compounds are applied, the district in which the plant is grown, the stage of the growth of the plant, the mode of application and various other factors, so that the compounds should be applied in an appropriate rate selected with due consideration for such factors. Generally, the compounds are applied at a rate of from 2 to 20,000 g per acre, preferably from 10 to 10,000 g per acre, as the effective ingredient.
While the concentration of the solution may vary in a considerably wide range, a concentration of generally from 0.001 to 100,000 ppm, preferably from 0.01 to 5,000 ppm, is employed.
The growth of plants treated with the plant growth regulating compositions of this invention was found to be accelerated as compared with untreated plants. In particular, the development of the root system and the increase of the fresh weight were remarkable, which would contribute to early-season harvests, and increased yields. For example, the application of the compositions to plants requiring transplantation such as rice plants encourages rooting and striking whereby highly stable harvests can be expected. The compositions of the present invention which exhibits remarkable activity under low temperature conditions are especially noteworthy in ensuring strong resistance of seedlings to the phenomenon of lowering of season average temperatures which is observed in recent years and is called "abnormal weather conditions".
In order to indicate more fully the nature and utility of this invention, the following specific examples of practice are set forth, it being understood that these examples are presented as illustrative only and not intended to limit the scope of the invention.
EXAMPLE 1
1 part of menadione sodium bisulfite, 1 part of Tween 20® (surfactant supplied by Kao Atlas K.K., Japan) and 98 parts of diatomaceous earth were thoroughly mixed to obtain a dust formulation.
EXAMPLE 2
A liquid formulation was prepared from 5 parts of 4-amino-2-methyl-1-naphthol hydrochloride and 95 parts of water.
EXAMPLE 3
10 parts of menadiol diacetate, 88 parts of clay and 2 parts of sodium dodecylbenzene sulfonate were thoroughly mixed to obtain a wettable powder.
EXAMPLE 4
The compounds of the present invention and the solid carriers listed in Table 1 were thoroughly mixed in the ratios set forth in the Table to obtain a dust formulation.
              TABLE 1                                                     
______________________________________                                    
              Part by              Part by                                
Compound      weight    Carrier    weight                                 
______________________________________                                    
menadione dimethyl-                                                       
              5         diatomaceous                                      
                                   50                                     
pryimidinol bisulfite   earth                                             
                        clay       45                                     
menadiol tetrasodium                                                      
              2         diatomaceous                                      
                                   40                                     
diphosphate             earth                                             
                        talc       58                                     
menadiol disodium                                                         
              2         talc       50                                     
disulfate               kaolin     48                                     
4-amino-3-methyl-1-                                                       
              2         talc       48                                     
naphthol hydrochloride                                                    
1,4-diamino-2-methyl-                                                     
              1         talc       99                                     
naphthalene dihydro-                                                      
chloride                                                                  
menadiol dinicotinate                                                     
              1         clay       99                                     
dihydrochloride                                                           
______________________________________
EXAMPLE 5
1 acre/400000 Neubauer's pots were each charged with a mixture of 500 g of soil, 3 g of Tomoe Kasei Special No.8 (fertilizer, N--P2 O5 --K2 O (6:7:7)) and a prescribed quantity of a dust formulation prepared as in Example 1. Each of the pots was seeded with 20 germination-hastened rice plant seeds which were then grown in a greenhouse at 25° C. for 15 days. Two runs of experiments were carried out respectively in the test plot and control plot. The plant lengths and main root lengths of the treated plants were measured to obtain the ratios thereof to those of the untreated plants. The results are shown in Table 2 below.
              TABLE 2                                                     
______________________________________                                    
                  Increase   Main Root                                    
Experimental Plot in Height (%)                                           
                             Length (%)                                   
______________________________________                                    
Untreated         100        100                                          
Treated                                                                   
dust formulation 0.5 g/pot                                                
                  109        108                                          
dust formulation 1 g/pot                                                  
                  132        122                                          
dust formulation 2 g/pot                                                  
                  109        115                                          
dust formulation 3 g/pot                                                  
                  100        110                                          
______________________________________                                    
 Note:                                                                    
 The average height and main root length of the untreated plants were 5.90
 cm and 7.56 cm, respectively
As is indicated in Table 2, the growths of the shoots or tops and roots of the plants treated with the dust formulation of the present invention were apparently accelerated.
EXAMPLE 6
Into 20-mm diam. test tubes were poured menadione sodium bisulfite solutions respectively having active ingredient concentrations of 10 ppm and 100 ppm. The second-leaf-stage seedlings of rice plants with the primary root thereof cut off except for the base portion 1 mm high were fixed with absorbent cotton around the stem portion thereof so that the seedlings would be disposed 1 cm below the surface of each solution. After growing the seedlings at 30° C. under continuous irradiation at 3,300 lux for 8 days, the maximum root lengths of the seedlings were measured to obtain the ratios thereof to those of the untreated seedlings. The results are set forth in Table 3.
              TABLE 3                                                     
______________________________________                                    
                  Max. root                                               
Concentration (ppm)                                                       
                  length (%)                                              
______________________________________                                    
Untreated         100                                                     
Treated                                                                   
 10               160                                                     
100               129                                                     
______________________________________                                    
 Note:                                                                    
 The average maximum root length of the untreated seedlings was 43.4 mm.
As is apparent from Table 3, the treatment with menadione sodium bisulfite solution encourages rooting of the rice plant seedlings.
EXAMPLE 7
Nursery boxes each of a size of 30×60×5 cm were filled with Pilomat® (medium for raising seedlings, supplied by Marusan Seishi K.K., Japan) as seedling beds, to which 4 g, 8 g and 16 g, respectively, of a dust formulation prepared as in Example 1 were added. Subsequently, each of the boxes was seeded with 210 g of germination-hastened paddy rice seeds (Sasanishiki) which were covered with soil for growing seedlings. The seedlings were caused to emerge at 32° C. for 2 days, greened at 25° C. for another 2 days, and then hardened in a greenhouse. 21 days after seeding, the traits of the young seedlings were examined, and the results shown in Table 4 were obtained.
On the same day, 4 seedlings per clump were transplanted into 1 acre/200000 pots which were placed in a biotron having a high temperature area (day/night temperatures: 25° C./17° C.) and a low temperature limit area (day/night temperatures: 17° C./12° C.) to promote striking 7 days after transplanting, the seedlings were sampled to examine the degree of striking. The data obtained by the striking tests in the high temperature area and the low temperature limit area are summarized respectively in Table 5 and Table 6.
              TABLE 4                                                     
______________________________________                                    
Traits of Young Seedlings                                                 
                              Dry                                         
                              Weight                                      
            Seedling Height   of tops                                     
                                     Number                               
Experimental Plot                                                         
            Age      (mm)     (mg)   of Roots                             
______________________________________                                    
Untreated   3.1      107.0    17.4   8.6                                  
Treated                                                                   
dust formulation                                                          
            3.2      102.0    18.8   9.9                                  
4 g/case                                                                  
dust formulAtion                                                          
            3.1      103.4    18.7   8.9                                  
8 g/case                                                                  
dust formulation                                                          
            3.1       99.4    17.5   9.4                                  
16 g/case                                                                 
______________________________________
As is apparent from Table 4, the seedlings treated with the dust formulation of the present invention were shorter in height than the untreated seedlings but were improved in dry weight of tops and number of roots.
              TABLE 5                                                     
______________________________________                                    
Striking Tests Under High Temperature Conditions                          
                           Total  Num-  Max.                              
                           Num-   ber of                                  
                                        Root                              
Experimental                                                              
         Seedling  Height  ber of Fresh Length                            
Plot     Age       (mm)    Roots  Roots (mm)                              
______________________________________                                    
Untreated                                                                 
         3.7       117.0   14.0   8.0   87.0                              
Treated                                                                   
dust formu-                                                               
         3.7       112.6   15.4   9.4   95.3                              
lation 4 g/                                                               
case                                                                      
dust formu-                                                               
         3.8       104.1   16.4   10.4  93.4                              
lation 8 g/                                                               
case                                                                      
dust formu-                                                               
         3.8       114.1   14.9   8.3   88.4                              
lation 16 g/                                                              
case                                                                      
______________________________________
As is seen from Table 5, the treated seedlings were improved in development of fresh roots and maximum root length in comparison with the untreated seedings.
              TABLE 6                                                     
______________________________________                                    
Striking Tests Under Low Temperature Conditions                           
                           Total  Num-  Max.                              
                           Num-   ber of                                  
                                        Root                              
Experimental                                                              
         Seedling  Height  ber of Fresh Length                            
Plot     Age       (mm)    Roots  Roots (mm)                              
______________________________________                                    
Untreated                                                                 
         3.2       112.9   13.0   4.4   20.7                              
Treated                                                                   
dust formu-                                                               
         3.1       107.6   12.0   6.6   12.9                              
lation 4 g/                                                               
case                                                                      
dust formu-                                                               
         3.3       105.6   12.8   7.1   31.6                              
lation 8 g/                                                               
case                                                                      
dust formu-                                                               
         3.2       109.3   14.8   8.5   32.9                              
lation 16 g/                                                              
case                                                                      
______________________________________
As is illustrated in Table 6, the number of fresh roots developed from the untreated seedlings was only 4.4, while those of fresh roots developed from the treated seedlings were 7 to 9 which were close to those observed under high temperature conditions. These data indicate that the treatment with the plant growth regulating compositions of the present invention is effective in encouraging rooting and striking at low temperatures.
EXAMPLE 8
Pots each of a size of 14 cm diam.×5 cm were filled with 500 g of garden soil each into which was injected 30 cc of a liquid formulation prepared as in Example 2 and diluted 500- and 5,000-fold, respectively. Thereafter, each of the pots was seeded with 20 seeds of Japanese radish (Ohkura Daikon) which were covered with soil. The radishes were grown in a greenhouse at 25° C. for 12 days, and the top weights thereof were measured to obtain the ratios between the weights of the treated and untreated radishes. The results are shown in Table 7.
              TABLE 7                                                     
______________________________________                                    
Experimental Plot                                                         
                Top weight (%)                                            
______________________________________                                    
Untreated       100                                                       
Treated                                                                   
liquid formulation                                                        
                111                                                       
diluted 500-fold                                                          
liquid formulation                                                        
                128                                                       
diluted 5,000-fold                                                        
______________________________________                                    
 Note:                                                                    
 The average top weight of the untreated radishes was 903 mg.
It is apparent from Table 7 that the treatment with the liquid formulation of the present invention is effective in accelerating the growth of the tops of the radishes.
EXAMPLE 9
Seedling cases each of a size of 5×15×10 cm were filled with 500 g of garden soil each into which was injected 30 cc of 4-amino-3-methyl-1-naphthol hydrochloride solutions having an active ingredient concentration of 10 ppm and 100 ppm, respectively. Each of the cases was then seeded with 15 seeds of spinach (Heianhiyoshimaru) which were covered with soil. The spinaches were grown in a greenhouse at 25° C. for 28 days, and the top weights thereof were measured to obtain the ratios between the weights of the treated and untreated spinaches. The results are set forth in Table 8.
              TABLE 8                                                     
______________________________________                                    
Concentration  Top Weight                                                 
(ppm)          (%)                                                        
______________________________________                                    
Untreated      100                                                        
Treated                                                                   
10             115                                                        
100            132                                                        
______________________________________                                    
 Note:                                                                    
 The average top weight of the untreated spinaches was 1.01 g.
It is to be noted from Table 8 that the treatment with 4-amino-3-methyl-1-naphthol hydrochloride solutions increases the top weights of spinaches.
EXAMPLE 10
Seedling cases each of a size of 5×15×10 cm were filled with 500 g of garden soil each into which was injected 30 cc of menadiol dinicotinate dihydrochloride solutions having an active ingredient concentration of 10 ppm and 100 ppm, respectively. The cases thus treated were each seeded with 15 seeds of Chinese cabbage (Ohzeki Hakusai) which were covered with soil. The Chinese cabbages were grown in a greenhouse at 25° C. for 14 days, and the top weights thereof were measured to obtain the ratios between the top weights of the treated and untreated Chinese cabbages. The results are shown in Table 9.
              TABLE 9                                                     
______________________________________                                    
Concentration  Top Weight                                                 
(ppm)          (%)                                                        
______________________________________                                    
Untreated      100                                                        
Treated                                                                   
10             109                                                        
100            123                                                        
______________________________________                                    
 Note:                                                                    
 The average top weight of the untreated Chinese cabbage was 611 mg.
It is apparent from Table 9 that the treatment with menadiol dinicotinate dihydrochloride solutions increases the top weights of Chinese cabbages.
EXAMPLE 11
Cut chrysanthemum stalks were soaked in menadione sodium bisulfite solutions having an active ingredient concentration of 1 ppm, 10 ppm and 100 ppm, respectively, for 24 hours, then were stuck into vermiculite and were left standing in a greenhouse at 25° C. for 14 days. The rooting of the chrysanthemums was examined to obtain the ratios thereof to the rooting of the untreated chrysanthemums. The results are tabulated below.
              TABLE 10                                                    
______________________________________                                    
               Rooting  Total Length of                                   
Concentration  Ratio    Fresh Roots                                       
(ppm)          (%)      (%)                                               
______________________________________                                    
Untreated      100      100                                               
Treated                                                                   
 1             105      110                                               
10             118      216                                               
100            141      492                                               
______________________________________                                    
 Note:                                                                    
 The average number of fresh roots and total length thereof developed in  
 the untreated chrysanthemums were 11 and 25 mm, respectively.
As is indicated in Table 10, the treatment with menadione sodium bisulfite solutions is effective in encouraging rooting of chrysanthemums.
EXAMPLE 12
1 acre/200000 Wagner's pots were each charged with a 1:1 mixture of river sand and mountain sand. In the pot was sodded lawn grass (Penncross bentgrass) which had been collected with a hole cutter, and the lower portion of its thatch stratum had been then cut off to trim the roots to equal length. On the next day and 2 weeks thereafter, the lawn grass was treated with 20 cc of menadione sodium bisulfite solutions having an active ingredient concentration of 10 ppm and 100 ppm, respectively, by applying to the foliage. One month after sodding, the growth state of the roots of the lawn grass was examined to obtain the ratios between the root weights of the treated and untreated lawn grass. The results are shown in Table 11. Meanwhile the tops were trimmed every other day.
              TABLE 11                                                    
______________________________________                                    
Concentration  Air-Dry Weight                                             
(ppm)          of Roots (%)                                               
______________________________________                                    
Untreated      100                                                        
Treated                                                                   
10             172                                                        
100            124                                                        
______________________________________                                    
 Note:                                                                    
 The untreated lawn grass was sprayed only with 20 cc of water, and the   
 airdry weight of the roots thereof was 117 mg.
The data given in Table 11 indicate that, by spraying menadione sodium bisulfite solutions, the growth of the roots of lawn grass is apparently accelerated.
EXAMPLE 13
Nursery boxes each of a size of 30×60×5 cm were filled with particulate soil for raising seedlings as seedling beds, which soil was then sterilized. The procedure of Example 6 was then followed except that each of the boxes was seeded with 200 g of rice plant seeds (Koshihikari) which had been soaked in menadione dimethyl pyrimidinol bisulfite solutions having an active ingredient concentration of 10 ppm, 100 ppm and 1,000 ppm, respectively, at 20° C. for 48 hours and further treated with tap water at 32° C. for 24 hours to hasten germination. The young seedlings obtained 20 days after seeding were found to have the traits shown in the following Table 12.
              TABLE 12                                                    
______________________________________                                    
Traits of Young Seedlings                                                 
                      Air-Dry   Air-Dry                                   
Concentration                                                             
            Height    Weight of Weight of                                 
(ppm)       (mm)      Tops (mg) Roots (mg)                                
______________________________________                                    
Untreated   160.4     17.4      3.4                                       
Treated                                                                   
 10         159.7     17.9      3.8                                       
100         161.3     17.7      4.7                                       
1000        157.4     17.3      4.8                                       
______________________________________
As is apparent from Table 12, the seed soaking treatment with menadione dimethyl pyrimidinol bisulfite solutions notably accelerates the growth of the roots of rice plants although the growth of the tops thereof was not appreciably different from that of the untreated rice plants.
EXAMPLE 14
1 acre/200000 Wagner's pots were each charged with 3 litres of 1 ppm aqueous solution of a compound of the present invention the pH of which had been adjusted to 5.0. Subsequently, floating nets were spread over the surfaces of the solutions which were seeded with 40 germination-hastened rice plant seeds (Nipponbare). The rice plants were grown in a greenhouse at 25° C. for 6 days, and the heights of the seedlings thus obtained and the main root lengths were measured to obtain the ratios thereof to those of the untreated rice plants. The results are summarized in Table 13.
              TABLE 13                                                    
______________________________________                                    
                   Increase in                                            
                             Main Root                                    
Compound           Height (%)                                             
                             Length (%)                                   
______________________________________                                    
4-amino-2-methyl-1-                                                       
                   185       184                                          
naphthol hydrochloride                                                    
Menadiol tetrasodium                                                      
                   162       149                                          
diphosphate                                                               
menadiol disodium disulfate                                               
                   145       138                                          
1,4-diamino-2-methyl-                                                     
                   129       152                                          
naphthalene dihydro-                                                      
chloride                                                                  
menadiol bis(glucoside                                                    
                   118       120                                          
tetraacetate)                                                             
______________________________________                                    
 Note:                                                                    
 The average height and main root length of the untreated rice plants were
 2.13 cm and 5.09 cm, respectively.
As is apparent from the above data, the growths of both the tops and the roots of the treated rice plants were accelerated.

Claims (9)

What is claimed is:
1. A method for accelerating the growth of plants which comprises applying to the foliage, roots, stems, and seeds of the plants and/or to the soil or other medium in which the plants are grown an effective plant growth accelerating amount of at least one water-soluble derivative of a vitamin K compound selected from the group consisting of
(1) a menadione bisulfite selected from menadione sodium bisulfite and menadione dimethylpyrimidinol bisulfite,
(2) a menadiol inorganic acid ester salt selected from menadiol tetrasodium diphosphate and menadiol disodium disulfate,
(3) menadiol dinicotinate dihydrochloride,
(4) menadiol bis(glucoside tetraacetate),
(5) 4-amino-2-methyl-1-naphthol hydrochloride,
(6) 4-amino-3-methyl-1-naphthol hydrochloride, and
(7) 1,4-diamino-2-methylnaphthalene dihydrochloride.
2. A method according to claim 1 wherein the water-soluble derivative of a vitamin K compound is a menadione bisulfite selected from menadione sodium bisulfite and menadione dimethylpyrimidinol bisulfite.
3. A method according to claim 1 wherein the water-soluble derivative of a vitamin K compound is a menadiol inorganic acid ester salt selected from menadiol tetrasodium diphosphate and menadiol disodium disulfate.
4. A method according to claim 1 wherein the water-soluble derivative of a vitamin K compound is a menadiol dinicotinate dihydrochloride.
5. A method according to claim 1 wherein the water-soluble derivative of a vitamin K compound is a menadiol bis(glucoside tetraacetate).
6. A method according to claim 1 wherein the water-soluble derivative of a vitamin K compound is a 4-amino-2-methyl-1-naphthol hydrochloride.
7. A method according to claim 1 wherein the water-soluble derivative of a vitamin K compound is a 4-amino-2-methyl-1-naphthol hydrochloride.
8. A method according to claim 1 wherein the water-soluble derivative of a vitamin K compound is a 1,4-diamino-2-methylnaphthalene dihydrochloride.
9. A method according to claim 1 wherein the water-soluble derivative of a vitamin K compound is a applied at a rate of from 2 to 20,000 g. per acre.
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Cited By (13)

* Cited by examiner, † Cited by third party
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EP0465907A1 (en) * 1990-06-27 1992-01-15 LUIGI STOPPANI S.p.A. Method and composition for stimulating the growth of vegetables
US5116406A (en) * 1989-06-20 1992-05-26 Mitsubishi Gas Chemical Company, Inc. Plant growth regulating composition
WO1995003702A1 (en) * 1993-07-29 1995-02-09 Consejo Superior Investigaciones Cientificas Compositions for inducing resistance to tracheomicosis in plants
WO1999012868A1 (en) * 1997-09-11 1999-03-18 Nonomura Arthur M Methods and compositions for enhancing growth of living organisms
US6258749B1 (en) 2000-02-22 2001-07-10 The Dow Chemical Company Methods for treating plants and enhancing plant growth using polyacylglycosides and/or polyalkylglycosides and formulations for same
US20050119127A1 (en) * 2003-12-02 2005-06-02 David Cambri Fertilizer composition to stimulate the absorption of nutritive substances in plants
ES2332494A1 (en) * 2008-08-04 2010-02-05 Consejo Superior De Investigaciones Cientificas (Csic) Use of menadione to increase saline stress tolerance in plants
WO2012045901A2 (en) 2010-10-06 2012-04-12 Consejo Superior De Investigaciones Científicas (Csic) Compositions for controlling the psyllids trioza erytreae and diaphorina citri, vectors of bacteria of the genus candidatus liberibacter, which cause the most serious known disease of citrus, namely huanglongbing (hlb)
WO2014152496A1 (en) * 2013-03-15 2014-09-25 KamTec, LLC Signaling compositions, methods, and systems for effecting plant growth and burndown, and enhancement of crops and herbicides
US8999890B2 (en) 2013-03-15 2015-04-07 KamTec, LLC Signaling compositions, methods, and systems for effecting plant burndown and herbicide enhancement
EP2862443A4 (en) * 2012-06-13 2015-12-16 Agro Stock S A Root-growth-promoting liquid formulation that enhances defence response in plants, and use of same
US9464283B2 (en) 2013-03-15 2016-10-11 KamTec, LLC Signaling compositions, methods, and systems for effecting plant growth and crop enhancement
US11464231B2 (en) * 2019-05-15 2022-10-11 Ilicitor LLC Composition for stimulating immune responses in plants

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US5116406A (en) * 1989-06-20 1992-05-26 Mitsubishi Gas Chemical Company, Inc. Plant growth regulating composition
EP0465907A1 (en) * 1990-06-27 1992-01-15 LUIGI STOPPANI S.p.A. Method and composition for stimulating the growth of vegetables
WO1995003702A1 (en) * 1993-07-29 1995-02-09 Consejo Superior Investigaciones Cientificas Compositions for inducing resistance to tracheomicosis in plants
WO1999012868A1 (en) * 1997-09-11 1999-03-18 Nonomura Arthur M Methods and compositions for enhancing growth of living organisms
US5958104A (en) * 1997-09-11 1999-09-28 Nonomura; Arthur M. Methods and compositions for enhancing plant growth
US6258749B1 (en) 2000-02-22 2001-07-10 The Dow Chemical Company Methods for treating plants and enhancing plant growth using polyacylglycosides and/or polyalkylglycosides and formulations for same
WO2001062088A2 (en) * 2000-02-22 2001-08-30 The Dow Chemical Company Safening high concentrations of phytocatalysts
WO2001062088A3 (en) * 2000-02-22 2002-03-14 Dow Chemical Co Safening high concentrations of phytocatalysts
US20050119127A1 (en) * 2003-12-02 2005-06-02 David Cambri Fertilizer composition to stimulate the absorption of nutritive substances in plants
EP1538136A1 (en) * 2003-12-02 2005-06-08 Valagro S.p.A. Fertilizer composition to stimulate the absorption of nutritive substances in plants
WO2005054156A1 (en) * 2003-12-02 2005-06-16 Valagro S.P.A. Fertilizer composition to stimulate the absorption of nutritive substances in plants
WO2010018281A1 (en) * 2008-08-04 2010-02-18 Consejo Superior De Investigaciones Científicas (Csic) Use of menadione to increase saline stress tolerance in plants
ES2332494A1 (en) * 2008-08-04 2010-02-05 Consejo Superior De Investigaciones Cientificas (Csic) Use of menadione to increase saline stress tolerance in plants
WO2012045901A2 (en) 2010-10-06 2012-04-12 Consejo Superior De Investigaciones Científicas (Csic) Compositions for controlling the psyllids trioza erytreae and diaphorina citri, vectors of bacteria of the genus candidatus liberibacter, which cause the most serious known disease of citrus, namely huanglongbing (hlb)
EP2625956A2 (en) * 2010-10-06 2013-08-14 Consejo Superior De Investigaciones Científicas (CSIC) Compositions for controlling the psyllids trioza erytreae and diaphorina citri, vectors of bacteria of the genus candidatus liberibacter, which cause the most serious known disease of citrus, namely huanglongbing (hlb)
CN103260405A (en) * 2010-10-06 2013-08-21 科学研究高级委员会 Compositions for controlling the psyllids trioza erytreae and diaphorina citri, vectors of bacteria of the genus candidatus liberibacter, which cause the most serious known disease of citrus, namely huanglongbing (hlb)
JP2013539752A (en) * 2010-10-06 2013-10-28 コンセホ・スペリオール・デ・インベスティガシオネス・シエンティフィカス Composition for controlling killer whales Triozaerytreae and Diaphorinactiri, which are bacterial vectors of the genus Candidasuliberibacter causing the most serious known citrus diseases, namely citrus greening disease (HLB)
EP2625956A4 (en) * 2010-10-06 2014-05-07 Consejo Superior Investigacion Compositions for controlling the psyllids trioza erytreae and diaphorina citri, vectors of bacteria of the genus candidatus liberibacter, which cause the most serious known disease of citrus, namely huanglongbing (hlb)
EP2862443A4 (en) * 2012-06-13 2015-12-16 Agro Stock S A Root-growth-promoting liquid formulation that enhances defence response in plants, and use of same
WO2014152496A1 (en) * 2013-03-15 2014-09-25 KamTec, LLC Signaling compositions, methods, and systems for effecting plant growth and burndown, and enhancement of crops and herbicides
US8999890B2 (en) 2013-03-15 2015-04-07 KamTec, LLC Signaling compositions, methods, and systems for effecting plant burndown and herbicide enhancement
US9464283B2 (en) 2013-03-15 2016-10-11 KamTec, LLC Signaling compositions, methods, and systems for effecting plant growth and crop enhancement
US10081805B1 (en) 2013-03-15 2018-09-25 KamTec, LLC Signaling compositions, methods, and systems for effecting plant growth and crop enhancement
US11464231B2 (en) * 2019-05-15 2022-10-11 Ilicitor LLC Composition for stimulating immune responses in plants

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